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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5 Pt 1
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pubmed:dateCreated |
1992-12-23
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pubmed:abstractText |
The properties of Ca(2+)-activated K+ currents and channels were characterized in pregnant rat myometrium in whole cell and cell-attached patches and in lipid bilayers. Membrane depolarization of cultured myometrial cells from a holding potential of -50 to +70 mV in 10-mV steps under voltage-clamp conditions (whole cell mode) activated K+ outward currents (IK). At +70 mV, in the presence of 0.2 mM external Ca2+, the amplitude and activation time constant of IK were 15.0 +/- 2.1 microA/microF and 1.5 +/- 0.2 ms, respectively. Addition of 1 microM A23187 to the external solution increased the current from a control value of 16.0 +/- 2.0 to 67.9 +/- 9.1 microA/microF. Charybdotoxin, a blocker of Ca(2+)-activated K (KCa) channels, and a low concentration of tetraethylammonium chloride (TEA; 1 mM) decreased the amplitude of IK by 47 and 62%, respectively. In cell-attached patches from these cells, 1 microM A23187 increased the open time probability of a 143 +/- 6.0 pS K+ channel. Incorporation of plasma membrane vesicles from pregnant myometrium into lipid bilayers resulted in one predominant type of K+ channel. The unitary conductance of the K+ channel was 326 +/- 9.0 pS in symmetrical 450 mM KCl. The channel activation was both voltage and Ca2+ dependent. TEA inhibited the channel activity with a dissociation constant (Kd) of 378 +/- 10 microM at -60 mV or 1,477 +/- 80 microM at +60 mV. The whole cell currents were found to be stimulated by isoproterenol, a beta-adrenergic agent.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adrenergic beta-Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Lipid Bilayers,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Tetraethylammonium,
http://linkedlifedata.com/resource/pubmed/chemical/Tetraethylammonium Compounds
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0002-9513
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
263
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
C1049-56
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1359792-Adrenergic beta-Agonists,
pubmed-meshheading:1359792-Animals,
pubmed-meshheading:1359792-Calcium,
pubmed-meshheading:1359792-Electrophysiology,
pubmed-meshheading:1359792-Female,
pubmed-meshheading:1359792-Lipid Bilayers,
pubmed-meshheading:1359792-Myometrium,
pubmed-meshheading:1359792-Potassium Channels,
pubmed-meshheading:1359792-Pregnancy,
pubmed-meshheading:1359792-Pregnancy, Animal,
pubmed-meshheading:1359792-Rats,
pubmed-meshheading:1359792-Rats, Sprague-Dawley,
pubmed-meshheading:1359792-Tetraethylammonium,
pubmed-meshheading:1359792-Tetraethylammonium Compounds
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pubmed:year |
1992
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pubmed:articleTitle |
Ca(2+)-activated K+ channels in pregnant rat myometrium: modulation by a beta-adrenergic agent.
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pubmed:affiliation |
Department of Biochemistry and Molecular Biology, University of Texas Medical School, Houston.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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